- Pedm52 [Search on AGR]
Mus musculus PHENOTYPE: Presumed homozygotes have spina bifida. [provided by MGI curators]
- m7Anu [Search on AGR]
Mus musculus PHENOTYPE: Mice homozygous for this mutation exhibit spina bifida and curled tail. [provided by MGI curators]
- Skax14 [Search on AGR]
Mus musculus PHENOTYPE: Heterozygous mice exhibit spina bifida and homozygous mice exhibit neural tube defects. [provided by MGI curators]
- m12Bei [Search on AGR]
Mus musculus PHENOTYPE: Mice homozygous for this ENU-induced mutation exhibit omphalocele, encephalomeningocele, limited spina bifida, and limb defects including oligodactyly. [provided by MGI curators]
- Itpk1 [Search on AGR]
Mus musculus PHENOTYPE: Some mice homozygous for a gene trap allele exhibit neural tube defects (exencephaly and spina bifida), growth retardation, kyphoscoliosis, and rib formation. [provided by MGI curators]
- Mut1170 [Search on AGR]
Mus musculus PHENOTYPE: Mice homozygous for a chemically and radiation induced allele exhibit early postimplantation lethality. Mice heterozygous for this allele exhibit very short tails and occasional spina bifida. [provided by MGI curators]
- atx-3 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Enables cysteine-type deubiquitinase activity. Involved in chemical synaptic transmission. Located in cytoplasm and nucleus. Expressed in coelomocyte; head; somatic nervous system; and tail neurons. Used to study Machado-Joseph disease. Human ortholog(s) of this gene implicated in Machado-Joseph disease and late onset Parkinson's disease. Is an ortholog of human ATXN3 (ataxin 3) and ATXN3L (ataxin 3 like).
- Cyp26a1 [Search on AGR]
Mus musculus PHENOTYPE: Homozygotes for targeted null mutations die during mid-late gestation and exhibit spina bifida, caudal agenesis, and abnormalities of the kidneys, urogenital tract, hindgut, cervical vertebrae, and rostral hindbrain. [provided by MGI curators]
- Trpm6 [Search on AGR]
Mus musculus PHENOTYPE: Mice homozygous for a knock-out allele exhibit embryonic and postnatal lethality with exencephaly, spina bifida occulta, and abnormal brain and facial development. Mice heterozygous for a knock-out allele exhibit some premature death and decreased serummagnesium. [provided by MGI curators]
- gpg2 [Search on AGR]
Mus musculus PHENOTYPE: Homozygotes for this ENU-induced mutation exhibit left-right patterning defects in pulmonary, cardiovascular, and stomach development, partial penetrance of micrognathia, exencephaly, spina bifida, polydactyly, edema, and abnormal eye morphology. [provided by MGI curators]